His main research concerns Genetics, Genome-wide association study, Single-nucleotide polymorphism, Allele and Schizophrenia. His Genetics study incorporates themes from Psychosis and Disease. The concepts of his Genome-wide association study study are interwoven with issues in SNP, Bipolar disorder, Meta-analysis, Genetic association and Genetic architecture.
His Single-nucleotide polymorphism research is multidisciplinary, incorporating perspectives in Adipose tissue and Genetic analysis. Hreinn Stefansson combines subjects such as Disease cluster, Population variation, Immunology and Genome with his study of Allele. His research in Schizophrenia intersects with topics in Autism and Bioinformatics.
Hreinn Stefansson spends much of his time researching Genetics, Genome-wide association study, Genetic association, Single-nucleotide polymorphism and Schizophrenia. His Genetics research is multidisciplinary, relying on both Psychosis and Disease. The various areas that Hreinn Stefansson examines in his Genome-wide association study study include Odds ratio, Internal medicine, Case-control study, Bipolar disorder and Genetic architecture.
His research on Genetic association frequently connects to adjacent areas such as Meta-analysis. His primary area of study in Single-nucleotide polymorphism is in the field of SNP. Within one scientific family, he focuses on topics pertaining to Copy-number variation under Schizophrenia, and may sometimes address concerns connected to Cognition.
The scientist’s investigation covers issues in Genome-wide association study, Genetics, Schizophrenia, Copy-number variation and Genetic association. His studies in Genome-wide association study integrate themes in fields like Genetic correlation, Bipolar disorder, Disease, Autism spectrum disorder and Genetic architecture. In most of his Genetics studies, his work intersects topics such as Schizophrenia.
His Schizophrenia research includes themes of HLA-DQB1 and Gene duplication. His research integrates issues of White matter, Diffusion MRI, Fractional anisotropy, Cognition and Autism in his study of Copy-number variation. His biological study spans a wide range of topics, including Oncology, Bioinformatics, Meta-analysis, Genetic etiology and Smoking initiation.
Hreinn Stefansson focuses on Genome-wide association study, Genetics, Schizophrenia, Copy-number variation and Genetic architecture. His study in Genome-wide association study is interdisciplinary in nature, drawing from both Bipolar disorder, Brain morphometry, Meta-analysis, Genetic association and Attention deficit hyperactivity disorder. His Genetic association research incorporates themes from Immunology, Major histocompatibility complex, Genetic predisposition and Haplotype.
His studies in Quantitative trait locus and Gene are all subfields of Genetics research. His Schizophrenia research includes elements of Gene duplication, FMR1 and Autism spectrum disorder. His work deals with themes such as White matter, Diffusion MRI, Fractional anisotropy, Fragile X syndrome and Autism, which intersect with Copy-number variation.
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Biological insights from 108 schizophrenia-associated genetic loci
Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Aiden Corvin;James T. R. Walters.
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes.
Struan F. A. Grant;Gudmar Thorleifsson;Inga Reynisdottir;Rafil Benediktsson.
Nature Genetics (2006)
Neuregulin 1 and Susceptibility to Schizophrenia
Hreinn Stefansson;Engilbert Sigurdsson;Valgerdur Steinthorsdottir;Soley Bjornsdottir.
American Journal of Human Genetics (2002)
Large recurrent microdeletions associated with schizophrenia
Hreinn Stefansson;Dan Rujescu;Sven Cichon;Olli P. H. Pietilainen.
Common variants conferring risk of schizophrenia
Hreinn Stefansson;Hreinn Stefansson;Roel A. Ophoff;Roel A. Ophoff;Roel A. Ophoff;Stacy Steinberg;Stacy Steinberg;Ole A. Andreassen.
Association between Microdeletion and Microduplication at 16p11.2 and Autism
Lauren A. Weiss;Yiping Shen;Joshua M. Korn;Joshua M. Korn;Dan E. Arking.
The New England Journal of Medicine (2008)
Variant of TREM2 associated with the risk of Alzheimer's disease
Thorlakur Jonsson;Hreinn Stefansson;Stacy Steinberg;Ingileif Jonsdottir.
The New England Journal of Medicine (2013)
Genome-wide association study identifies five new schizophrenia loci
Stephan Ripke;Alan R. Sanders;Kenneth S. Kendler;Douglas F. Levinson.
Nature Genetics (2011)
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
Paul Hollingworth;Denise Harold;Rebecca Sims;Amy Gerrish.
Nature Genetics (2011)
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease.
Thorgeir E Thorgeirsson;Frank Geller;Patrick Sulem;Thorunn Rafnar.
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